Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C3715128
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1 		5 0 3 0.30 0 0
CUI: C3875492
Disease: Hypocalciuric hypercalcemia
Hypocalciuric hypercalcemia 		5 0 3 0.30 0 0
CUI: C4552089
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME 		5 0 3 0.30 0 0
CUI: C0345406
Disease: Neonatal hyperparathyroidism
Neonatal hyperparathyroidism 		2 0 2 0.25 0 0
CUI: C0865171
Disease: parathyroiditis
parathyroiditis 		2 0 2 0.25 0 0
CUI: C0342634
Disease: Neonatal hypocalcemia
Neonatal hypocalcemia 		3 0 2 0.22 0 0
CUI: C1840334
Disease: Hypoparathyroidism, Autosomal Recessive
Hypoparathyroidism, Autosomal Recessive 		3 0 2 0.22 0 0
CUI: C0151714
Disease: Hypermagnesemia
Hypermagnesemia 		10 0 3 0.20 0 0
CUI: C0729198
Disease: Decreased circulating parathyroid hormone level
Decreased circulating parathyroid hormone level 		4 0 2 0.20 0 0
CUI: C4551961
Disease: Familial Isolated Hyperparathyroidism
Familial Isolated Hyperparathyroidism 		10 0 3 0.20 0 0
CUI: C0006705
Disease: Calcium Metabolism Disorders
Calcium Metabolism Disorders 		5 0 2 0.18 0 0
CUI: C1455734
Disease: Congenital hypoparathyroidism
Congenital hypoparathyroidism 		5 0 2 0.18 0 0
CUI: C0342345
Disease: Hypoparathyroidism - autosomal dominant
Hypoparathyroidism - autosomal dominant 		12 44 3 0.18 1 2.0E-02
CUI: C2673443
Disease: Hypermagnesiuria
Hypermagnesiuria 		6 0 2 0.17 0 0
CUI: C1832615
Disease: HYPERPARATHYROIDISM, NEONATAL SEVERE
HYPERPARATHYROIDISM, NEONATAL SEVERE 		14 0 3 0.16 0 0
CUI: C0271846
Disease: Familial hyperparathyroidism
Familial hyperparathyroidism 		7 0 2 0.15 0 0
CUI: C1522135
Disease: Hypermagnesemia result
Hypermagnesemia result 		7 0 2 0.15 0 0
CUI: C4554647
Disease: Hypermagnesemia, CTCAE
Hypermagnesemia, CTCAE 		7 0 2 0.15 0 0
CUI: C0020599
Disease: Hypocalciuria
Hypocalciuria 		16 0 3 0.14 0 0
CUI: C0085622
Disease: Monoplegia
Monoplegia 		1 0 1 0.12 0 0
CUI: C0154693
Disease: Hemiplegia, Flaccid
Hemiplegia, Flaccid 		1 0 1 0.12 0 0
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		1 0 1 0.12 0 0
CUI: C0271848
Disease: Hyperparathyroidism due to vitamin D deficiency
Hyperparathyroidism due to vitamin D deficiency 		1 0 1 0.12 0 0
CUI: C0332977
Disease: Congenital hemangiomatosis
Congenital hemangiomatosis 		1 0 1 0.12 0 0
CUI: C0346405
Disease: Ectopic parathyroid adenoma
Ectopic parathyroid adenoma 		1 0 1 0.12 0 0